# Medotech A/S

- Location (FDA's records): Westminster, CO
- FDA decisions: 2 (2010–2012): 2 510(k) clearances
- Product codes: KZM (1), HCC (1)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- S.L.P., Ltd.: 2 (https://510kreport.com/company/slp)
- Myotronics-Noromed, Inc.: 1 (https://510kreport.com/company/myotronics-noromed)
- Cole & Associates: 1 (https://510kreport.com/company/cole-associates)

## Firms that cite its devices most
- Sunstar Suisse S.A.: 1 (https://510kreport.com/company/sunstar-suisse)

## Its most-cited devices
- K092675: Grindcare (2010), cited by 2

## Recent decisions
- K113677: Grindcare Measure (Apr 5, 2012)
- K092675: Grindcare (Mar 3, 2010)

Source page: https://510kreport.com/company/medotech-a-s